Ventilatory control of the ‘isocapnic buffering’ region in rapidly-incremental exercise

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Abstract

During incremental exercise PCO2 does not fall for several work rates (‘isocapnic buffering’) above the anaerobic threshold (θan). We explored this apparent lack of compensatory hyperventilation in 24 normal subjects who underwent incremental cycling (15 W/min) to exhaustion. Ventilation, pulmonary gas exchange, and end-tidal gas tensions were computed breath-by-breath. In 10 subjects, arterial blood was sampled every 2 min throughout the test. Our findings confirmed the ‘isocapnic’ supra-θan region, but it consistently followed a progressive increase of PETCO2 in the sub-θan region. A similar pattern was evident for PaCO2. The leveling-out of PetCO2 and PaCO2 was a result of breathing frequency increasing at θan, thereby shortening expiratory time, i.e., progressively truncating the continued increase in the alveolar PCO2 slope. Consequently ‘isocapnic buffering’ during incremental exercise does not reflect PCO2 which continues to be regulated at a constant sub-θan value. Rather it reflects a ventilatory response to the metabolic acidosis which levels a systematically-rising phase of PetCO2 and PaCO2, largely through a change in breathing pattern. Respiratory compensation, as reflected by a declining PetCO2 and PaCO2, does not occur typically for a subsequent 2 or more minutes.

References (25)

  • E.M. Hey et al.

    Effects of various respiratory stimuli on the depth and frequency of breathing in man

    Respir. Physiol.

    (1966)
  • C. Olsen

    An enzymatic fluorimetric micromethod for determination of aceto-acetate, β-hydroxybutyrate, pyruvate and lactate

    Clin. Chim. Acta

    (1971)
  • C.J. Allen et al.

    Rate of change of alveolar carbon dioxide and the control of ventilation during exercise

    J. Physiol. (London)

    (1984)
  • E. Asmussen

    Muscular exercise

  • W.L. Beaver et al.

    Breath-by-breath measurement of true alveolar gas exchange

    J. Appl. Physiol.

    (1981)
  • G. Cumming

    Alveolar ventilation: recent model analysis

  • A.D. Edwards et al.

    The effect of increased lung volume on the expiratory rate of rise of alveolar carbon dioxide tension in normal man

    J. Physiol. (London)

    (1983)
  • L.J. Folinsbee et al.

    Respiratory patterns and control during unrestrained human running

  • T.S. Griffiths et al.

    Influence of peripheral chemoreceptors on the dynamics of the exercise hyperpnœa in man

    J. Physiol. (London)

    (1986)
  • J.E. Hansen et al.

    Predicted values for clinical exercise testing

    Am. Rev. Respir. Dis.

    (1984)
  • N.L. Jones

    Exercise testing in pulmonary evaluation: rationale, methods and the normal respiratory response to exercise

    N. Engl. J. Med.

    (1975)
  • N. Lamarra et al.

    Pulmonary gas exchange dynamics and blood gas regulation in incremental exercise

    J. Appl. Physiol.

    (1988)
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      An increase in lactate concentration occurs during the incremental exercise test due to anaerobic metabolism added to aerobic metabolism that exceeds VT. The process of lactate production produces H+ and decreases pH; however, for about 2 min after exceeding VT, it is first buffered by HCO3− in the body (Wasserman et al., 2017; Whipp et al., 1989). The period of isocapnic buffering is set up as a gradual increase in ventilation due to CO2 production associated with buffering of HCO3−; after this period, the progression of metabolic acidosis provokes hyperventilation.

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    Present address: Laboratory of Applied Physiology, California State University, Long Beach, CA 90840, U.S.A.

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